Long QT Syndrome: Difference between revisions
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m (New page: Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane portion of the ion channel protein and the degree of ion channel dysfu...) |
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Revision as of 08:02, 15 May 2007
Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane
portion of the ion channel protein and the degree of ion channel dysfunction caused by the mutations are important
independent risk factors influencing the clinical course of this disorder.[1]